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- Scorpion Therapeutics in Pleasant Prairie, WI, is seeking a QA professional for night shift responsibilities, ensuring compliance with GMP standards. This role involves oversight of operations, mentoring personnel, and resolving quality issues. Candidates must have a bachelor...SuggestedNight shift
- Lonza Inc. is seeking an LSA QA Sr. Compliance Specialist in Portsmouth, VA. The ideal candidate will have extensive experience in Quality Assurance within a GMP-regulated environment, leading quality review boards and ensuring compliance with internal procedures. This...Suggested
$118k - $145k
Catalent Pharma Solutions, located in Harmans, Maryland, is seeking a Lead Specialist in Client QA responsible for QA support and oversight of client projects from start to finish in GMP manufacturing. This role demands strong technical knowledge and the ability to work in a...Suggested- ...requirements, lead deviation investigations, and validate testing methods. The ideal candidate has over 10 years of experience in a GMP environment and possesses excellent problem-solving and leadership capabilities. This role requires collaboration with various departments...Suggested
$195k - $225k
...Director, US Commercial QA Lead (GMP) Quality Assurance – Hybrid/Remote – US (Greater Boston area) Pharvaris is a Nasdaq listed late-stage biotech company developing bradykinin B2 receptor antagonists for bradykinin-mediated diseases, with offices in Switzerland...SuggestedWork at officeRemote workFlexible hours2 days per week1 day per weekPharvaris
Lexington, MA2 days ago- GMP Quality Assurance Associate needs 5+ years of GMP Quality Control Laboratory knowledge and/or experience in API or finished product manufacturing, QA or Engineering. GMP Quality Assurance Associate requires: BS in a science-related field such as Pharmacy, Chemistry...Suggested
- The American Red Cross is hiring for a QA/QC position in Charlotte, NC. The role involves monitoring record processes, ensuring compliance... ...of 3 years' experience in QA, QC or similar fields within a GMP environment are required. Excellent analytical and problem-solving...Suggested
$48k - $52k
...manufacturing processes. The role includes reviewing compliance with corporate SOPs and FDA guidelines, performing inspections, and monitoring GMP compliance. Qualified candidates should hold a Bachelor’s degree and possess 2 years of relevant experience in Quality Assurance or...Suggested- ...exempt position that is responsible for day-to-day Quality Assurance (QA) activities to ensure continuous manufacturing and production of... ...regulations, specifications and certifications. Conducts GMP inspections of facilities and equipment, completes process monitoring...SuggestedFull timeWork experience placementWork at office
- A dietary supplement manufacturer in Hawaii is seeking a full-time Quality Assurance (QA) professional. Responsibilities include conducting GMP inspections, ensuring compliance with FDA regulations, and maintaining records. The ideal candidate should possess an Associate...SuggestedFull timeWork at office
- Unicon Pharma Inc is seeking a QA Inspector in the Town of Florida, New York. The role involves performing AQL inspections, reviewing manufacturing records, and ensuring compliance with GMP and company procedures. Qualified candidates should have a High School Diploma...Suggested
- ...QA/RA Specialist - Pharmaceutical GLP/GMP Experience Synergy is seeking a knowledgeable and meticulous QA/RA Specialist with strong expertise in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) within the pharmaceutical industry. The specialist...Suggested
Synergy Services
Dallas, TX13 hours ago $100 - $125 per hour
...Director, GMP Quality Assurance Location : Remote Employment Type : Contract (9-12 months+) Hourly Rate - $100-125HR Scientific... ..., GMP Quality Assurance to provide strategic and operational QA leadership supporting biologics manufacturing, analytical testing...SuggestedHourly payContract workRemote workAfternoon shiftScientific Search
New York, NY1 day ago- ...Co. KGaA seeks a Quality Assurance Manager for their Wilson, North Carolina facility. The role involves managing QA activities to ensure compliance with GMP and the timely release of manufacturing batches. Responsibilities include oversight of manufacturing processes, review...Suggested
- ...QA Lead Coordinator 6+ Month Contract Payrate- Upto $52/hr- $55/hr on W2 Location- Port Neches TX Top Must-Have Skills: • Chem Manufacturing experience • Advanced knowledge in GMP requirements and ISO standards • Ability to Lead/manage Quality Assurance...SuggestedContract workLocal area
Hillview Consulting Solutions
Port Neches, TX13 hours ago $70 - $80 per hour
...ensuring compliance with regulatory requirements. The ideal candidate will have a Bachelor’s degree in a relevant field and experience in GMP-regulated environments. The position offers a pay range of $70-$80 per hour and focuses on maintaining high-quality standards in...Hourly pay$270k - $300k
We are seeking an Executive Director of GMP Quality Assurance (QA) to serve as a senior quality leader responsible for developing, leading, and executing the global GMP QA strategy in support of a transition from clinical development to commercial readiness. This role ensures...GQR
San Diego, CA1 day ago$55k - $86.9k
KBI Biopharma Inc. is looking for a QA Specialist II in Durham, North Carolina. This role involves supporting the Manufacturing process in a GMP environment, ensuring compliance with quality standards, and providing real-time guidance to the Manufacturing team. Candidates...Shift work- ...Job Title: Quality Assurance Specialist – GMP / Medical Devices Job Location: Foster City, California Job Duration: 12 months Onsite Position: Foster City - 5 days/week - Local Candidates The Device Engineering team is seeking a qualified individua l to...Contract workLocal area
Cube Hub Inc.
Foster, CA1 day ago $40 - $45 per hour
...A well-known biopharmaceutical company is seeking a remote QA Specialist for a short-term contract. This role involves leading deviation investigations and writing CAPAs, requiring 4 to 7 years of GMP quality assurance experience. Candidates should have hands-on experience...Hourly payTemporary workRemote workJCW Group
New York, NY4 days ago- KBI Biopharma in Durham, NC, is looking for a Manufacturing Quality Assurance (MQA) Specialist to support the GMP manufacturing process. Responsibilities include on-floor compliance review, collaboration with manufacturing and laboratory departments, and execution of quality...Shift work
- Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical development and testing processes. The QA Specialist will be responsible...
- An established industry player is seeking a meticulous QA Associate to ensure product quality in a regulated environment. This role involves... ...in biology or chemistry, along with relevant experience in a GMP setting. Join a dynamic team where your contributions will...Night shift
- ...regulatory standards. Responsibilities include reviewing quality documentation, collaborating with various departments, and maintaining GMP practices. Ideal candidates have a Bachelor's degree, at least 2 years of relevant experience, and familiarity with industry systems....
- ...ChangeControl Productreworkandretrieval(mockrecall) Audit&Compliance Leadtheinternalauditprogramandcoordinateexternalaudits,includingISO,GMP,andcustomeraudits. Ensureauditreadinessanddrivecorrectiveactionsfromauditfindings. Qualification&Calibration...
- A leading pharmaceutical company is seeking a GMP Quality Assurance Associate in Indianapolis, Indiana. The role requires over 5 years of GMP Quality Control Laboratory experience and proficiency in quality systems, particularly in the context of pharmaceutical manufacturing...
$147k - $180k
...Quality Assurance team, responsible for quality oversight of external GMP manufacturers (CMOs/CDMOs) supporting commercial drug substance,... ...have experience managing commercial external manufacturers and QA review of batch documentation and quality events* Must have...Minimum wageFull timeFor contractorsLocal areaFlexible hours- KBI Biopharma in Durham, NC is seeking a Principal QA Specialist responsible for compliance review of Biopharmaceutical GMP data. This role includes reviewing test data, supporting client audits, and providing QA oversight of laboratory activities. The ideal candidate...
- ...Functions: Purpose: Provide strategic and enterprise-level leadership of GMP Quality and Quality across GxP domains, through oversight of a... ...and facilitate development opportunities and mentor and coach QA team members. Build and lead a high-performing GMP and QMS...Contract workImmediate start
- ...conducting internal audits, and maintaining quality databases. The ideal candidate should hold a relevant degree and have significant GMP experience. This full-time, on-site role entails mentoring colleagues and enhancing quality culture within the team. #J-18808-Ljbffr...Full time
